FOR LABORATORIESPharmacogenetic reporting, fully automated.
For laboratories that carry out pharmacogenetic analyses themselves. With the iGene PGx platform, delivering the raw results becomes faster and better: they are automatically converted into clear results with dosage advice, according to the current guidelines of CPIC and DPWG. This way, reporting is set up much faster than with its own reporting tool, and doctors and pharmacists receive a report they can continue with directly.
From genotype to dosage advice, without manual work.
Converting a genotype into correct dosage advice takes a lot: determining the metaboliser status, consulting the clinical guidelines and validating the gene-drug interactions. Per report, this costs analysts hours, time that could also go to more lab tests.
The iGene PGx platform takes over that work. As soon as the genotyping is complete, the raw data is converted into a validated, clinically relevant report, structured and easy to read for doctors and pharmacists.
What the platform delivers
- Genotyping and phenotyping, whether for one enzyme or twenty
- Dosage advice for 60+ medicines, according to CPIC and DPWG
- Clinical safety warnings when prescribing and dispensing
- Reports as PDF, in a patient app or directly in the electronic patient record
From lab data to report in three steps.
Without changes to the laboratory’s IT.
- Import lab dataThe laboratory imports the raw lab data in its existing format (VCF, PLINK, CSV, TXT, XLS and more), or the systems are linked for an automatic, secure transfer.
- Convert into adviceThe platform determines genotype and phenotype and links them to current science and the guidelines of CPIC and DPWG.
- Immediately usableThe reportThe results go directly to the healthcare provider’s electronic patient record, to a patient app or as a PDF report.
One partner for complete pharmacogenetic reporting.
- Always currentIf the CPIC or DPWG guidelines change, the advice is updated. This keeps the advice current, supported by thousands of studies.
- Fits the way of workingThe platform adapts to the processes, tools and systems of the laboratory, not the other way round. Plug-and-play, and so quickly operational.
- Under its own nameReports and apps for patients in understandable language, in the house style of the laboratory.
- Privacy and complianceISO 27001 certified and GDPR compliant, designed for healthcare. DNA data is kept strictly separate from personal data.
From practice.
Pharmacogenetic profiles for Erasmus MCErasmus MC uses the platform to convert DNA data in real time into pharmacogenetic reports for GPs, specialists and medical institutions.Read the case (English) ↗
The Pharmacogenetic Passport from GamediGamedi, a provider of diagnostic tests, launched the Gamedi Pharmacogenetic Passport with iGene, so that healthcare providers can tailor prescriptions to the patient.Read the case (English) ↗Good to know.
Can variants outside the panel also be tested?
Yes, with customisation. iGene is happy to discuss which variants the laboratory wants to test, and supports it in doing so.
How do the results reach patients and healthcare providers?
For patients, iGene makes apps and PDF reports, in understandable language and in the house style of the laboratory. Healthcare providers receive the results directly in their electronic patient record via an integration.
Is experience with pharmacogenetics needed?
No. The platform translates the lab data into clear advice. For questions, the pharmacogenetic experts of iGene help, via a dedicated support number and email address.
Is iGene certified?
Yes. iGene is ISO 27001 certified. All genetic analyses by iGene are carried out in an ISO 15189-accredited laboratory, with saliva kits from DNA Genotek (ON-500 and ON-600), produced in accordance with ISO 13485.
Curious what DNA analysis can mean in practice?
See per profession how the collaboration begins: for practitioners, pharmacies and laboratories.